Trisomy 13 - mitotic nondisjunction mosaicism 205620000
SNOMED CT code
| SNOMED code | 205620000 |
|---|---|
| name | Trisomy 13 - mitotic nondisjunction mosaicism |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Trisomy 13 - mitotic nondisjunction mosaicism (disorder) |
| synonyms | Trisomy 13 - mitotic nondisjunction mosaicism |
| attributes - group1 | |
| Associated morphology | Chromosome mosaicism 11704001 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 13 55401003 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Chromosome pair 13 55401003 |
| Associated morphology | Trisomy 78989007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Trisomy and partial trisomy of autosome 270521004 Complete trisomy 13 syndrome 21111006 Trisomy 13 - mitotic nondisjunction mosaicism 205620000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Trisomy and partial trisomy of autosome 270521004 Whole chromosome trisomy - mitotic nondisjunction mosaicism 254270008 Trisomy 13 - mitotic nondisjunction mosaicism 205620000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Trisomy 13 - mitotic nondisjunction mosaicism 205620000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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